This highly interactive half-day workshop is designed specifically for non-regulatory professionals to build a practical, real-world understanding of how regulation shapes product development, marketing, and post-market activity.
Through engaging case studies and hands-on activities, participants will demystify the medical device regulatory landscape.
Most importantly, the session equips attendees with the confidence, language, and tools to work more effectively with regulatory teams, asking better questions, spotting issues earlier, and strengthening cross-functional collaboration to improve outcomes.
To maximise access, this workshop will be offered in two identical sessions, choose:
info@wilam.comAn initiative ofBioMelbourne NetworkLevel 6, HWT Tower40 City RoadSouthbank, VIC 3006
Wilam means home in the Woi-wurrung language of the Wurundjeri People of the Kulin Nation, the Traditional Owners of the lands on which we are based.We respectfully acknowledge the Traditional Custodians of the unceded lands and waters of Victoria, the Bunurong, Eastern Maar, Gunaikurnai, Wadawurrung and Wurundjeri Woi-wurrung peoples, on which we live and work. We pay respect to their Elders past and present. We acknowledge the significant contribution that they and other Aboriginal and Torres Strait Islander people have made and continue to make to the research and knowledge systems that inform our community and our sector. We acknowledge that Aboriginal and Torres Strait Islander people continue to live in a spiritual and sacred relationship with this country and recognise our responsibility to continue to work towards reconciliation.